Regulatory Affairs Trainee

About the role

At Alcon, a global leader in eye care, we are looking for a Regulatory Affairs Trainee to support our regulatory team in Spain. You will gain hands‑on experience with medical device and medicinal product registration, documentation and post‑approval activities.

Key responsibilities

• Support medical device notification and registration activities with the Spanish Agency of Medicines and Medical Devices (AEMPS).
• Collect and prepare regulatory documentation for medical devices and medicinal products required for tender submissions.
• Coordinate the translation of medical device labeling materials.
• Review medical device labeling for the Surgical and Vision Care product portfolios.
• Support post‑approval regulatory activities for medicinal products, mainly related to variations.

Required profile

• Initiative and proactivity.
• Integrity and trust.
• Teamwork and collaboration.
• Results orientation.
• Planning and alignment skills.
• Adaptability.
• Good written and spoken English.
• Currently pursuing or recently completed a Master’s or postgraduate degree in Pharmacy, Chemistry, Biology or related health/life sciences.